Watanabe Y - Search Results

1

Roles of specific cytokines in bone remodeling and hematopoiesis in Gaucher disease.

Yoshino M, Watanabe Y, Tokunaga Y, Harada E, Fujii C, Numata S, Harada M, Tajima A, Ida H. Yoshino M, et al. Among authors: watanabe y. Pediatr Int. 2007 Dec;49(6):959-65. doi: 10.1111/j.1442-200X.2007.02502.x. Pediatr Int. 2007. PMID: 18045304

2

Effect of supplementation with L-carnitine at a small dose on acylcarnitine profiles in serum and urine and the renal handling of acylcarnitines in a patient with multiple acyl-coenzyme A dehydrogenation defect.

Yoshino M, Tokunaga Y, Watanabe Y, Yoshida I, Sakaguchi M, Hata I, Shigematsu Y, Kimura M, Yamaguchi S. Yoshino M, et al. Among authors: watanabe y. J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Jul 15;792(1):73-82. doi: 10.1016/s1570-0232(03)00310-6. J Chromatogr B Analyt Technol Biomed Life Sci. 2003. PMID: 12828999

3

Late-onset ornithine transcarbamylase deficiency in male patients: prognostic factors and characteristics of plasma amino acid profile.

Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M. Harada E, et al. Among authors: watanabe y. Pediatr Int. 2006 Apr;48(2):105-11. doi: 10.1111/j.1442-200X.2006.02181.x. Pediatr Int. 2006. PMID: 16635166

4

Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency.

Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T, Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M, Watanabe Y, Inokuchi T, Yokoyama T, Kiwaki K, Nakamura K, Endo F, Tsuchiya S, Ohura T. Uematsu M, et al. Among authors: watanabe y. J Hum Genet. 2007;52(12):1040-1043. doi: 10.1007/s10038-007-0211-9. Epub 2007 Oct 30. J Hum Genet. 2007. PMID: 17968484

5

Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients.

Numata S, Harada E, Maeno Y, Ueki I, Watanabe Y, Fujii C, Yanagawa T, Takenaka S, Inoue T, Inoue S, Goushi T, Yasutake T, Mizuta T, Yoshino M. Numata S, et al. Among authors: watanabe y. J Hum Genet. 2008;53(1):10-17. doi: 10.1007/s10038-007-0212-8. Epub 2007 Nov 20. J Hum Genet. 2008. PMID: 18030415

6

Various types of LRP5 mutations in four patients with osteoporosis-pseudoglioma syndrome: identification of a 7.2-kb microdeletion using oligonucleotide tiling microarray.

Narumi S, Numakura C, Shiihara T, Seiwa C, Nozaki Y, Yamagata T, Momoi MY, Watanabe Y, Yoshino M, Matsuishi T, Nishi E, Kawame H, Akahane T, Nishimura G, Emi M, Hasegawa T. Narumi S, et al. Among authors: watanabe y. Am J Med Genet A. 2010 Jan;152A(1):133-40. doi: 10.1002/ajmg.a.33177. Am J Med Genet A. 2010. PMID: 20034086

7

[Phenylketonuria--toward a better carry-over care].

Yoshino M, Watanabe Y, Ohira T, Harada N. Yoshino M, et al. Among authors: watanabe y. Nihon Rinsho. 2010 Jan;68(1):123-6. Nihon Rinsho. 2010. PMID: 20077803 Review. Japanese.

8

A familial case of LEOPARD syndrome associated with a high-functioning autism spectrum disorder.

Watanabe Y, Yano S, Niihori T, Aoki Y, Matsubara Y, Yoshino M, Matsuishi T. Watanabe Y, et al. Brain Dev. 2011 Aug;33(7):576-9. doi: 10.1016/j.braindev.2010.10.006. Epub 2010 Nov 18. Brain Dev. 2011. PMID: 21093184

9

Coagulopathy in patients with late-onset ornithine transcarbamylase deficiency in remission state: a previously unrecognized complication.

Ihara K, Yoshino M, Hoshina T, Harada N, Kojima-Ishii K, Makimura M, Hasegawa Y, Watanabe Y, Yamaguchi S, Hara T. Ihara K, et al. Among authors: watanabe y. Pediatrics. 2013 Jan;131(1):e327-30. doi: 10.1542/peds.2012-0030. Epub 2012 Dec 3. Pediatrics. 2013. PMID: 23209112

10

Fatigue and quality of life in citrin deficiency during adaptation and compensation stage.

Okano Y, Kobayashi K, Ihara K, Ito T, Yoshino M, Watanabe Y, Kaji S, Ohura T, Nagao M, Noguchi A, Mushiake S, Hohashi N, Hashimoto-Tamaoki T. Okano Y, et al. Among authors: watanabe y. Mol Genet Metab. 2013 May;109(1):9-13. doi: 10.1016/j.ymgme.2013.01.020. Epub 2013 Feb 9. Mol Genet Metab. 2013. PMID: 23453692

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